{"title":"Triazoles synthesis using nanocatalyst triazine-pyrimidine-modified cobalt-based metal-organic frameworks.","authors":"Mahtab Amirian, Ramin Ghorbani-Vaghei, Sedigheh Alavinia","doi":"10.1039/d5na00299k","DOIUrl":null,"url":null,"abstract":"<p><p>This research introduces a recyclable and environmentally friendly catalyst, Co(BDC-NH<sub>2</sub>)-TA-PY, for the efficient synthesis of triazoles <i>via</i> the reaction of benzaldehydes, nitromethane, and sodium azide. The synthesis of Co(BDC-NH<sub>2</sub>)-TA-PY was carried out through the post-synthetic modification of Co(BDC-NH<sub>2</sub>), incorporating triazine-pyrimidine (TA-PY) functional groups. The key advantage of this catalyst lies in its dual functionality: the Lewis acidic sites of the Co(BDC-NH<sub>2</sub>) metal-organic framework (MOF) are complemented by the Brønsted basic sites of the triazine and pyrimidine groups. This study represents the first example of a post-synthetic modification of the Co(BDC-NH<sub>2</sub>) metal-organic framework (MOF) by integrating triazine and pyrimidine functional groups, which significantly enhanced its catalytic performance. The abundant TA-PY ligand increased the catalytic activity from 42% to 94%. Co(BDC-NH<sub>2</sub>) nanocrystals were successfully synthesized and characterized, exhibiting a highly crystalline structure. Following the post-synthetic modification to synthesize Co(BDC-NH<sub>2</sub>)-TA-PY, the catalyst retained its uniform morphology, ensuring consistent structural integrity. Furthermore, the structural integrity, morphology, and chemical composition of the reused Co(BDC-NH<sub>2</sub>)-TA-PY were thoroughly examined, revealing no significant differences between the fresh and reused catalysts. These results highlight the potential of functionalized cobalt-based metal-organic frameworks as versatile and sustainable catalysts for broader organic reactions.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" ","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12301849/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanoscale Advances","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d5na00299k","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
This research introduces a recyclable and environmentally friendly catalyst, Co(BDC-NH2)-TA-PY, for the efficient synthesis of triazoles via the reaction of benzaldehydes, nitromethane, and sodium azide. The synthesis of Co(BDC-NH2)-TA-PY was carried out through the post-synthetic modification of Co(BDC-NH2), incorporating triazine-pyrimidine (TA-PY) functional groups. The key advantage of this catalyst lies in its dual functionality: the Lewis acidic sites of the Co(BDC-NH2) metal-organic framework (MOF) are complemented by the Brønsted basic sites of the triazine and pyrimidine groups. This study represents the first example of a post-synthetic modification of the Co(BDC-NH2) metal-organic framework (MOF) by integrating triazine and pyrimidine functional groups, which significantly enhanced its catalytic performance. The abundant TA-PY ligand increased the catalytic activity from 42% to 94%. Co(BDC-NH2) nanocrystals were successfully synthesized and characterized, exhibiting a highly crystalline structure. Following the post-synthetic modification to synthesize Co(BDC-NH2)-TA-PY, the catalyst retained its uniform morphology, ensuring consistent structural integrity. Furthermore, the structural integrity, morphology, and chemical composition of the reused Co(BDC-NH2)-TA-PY were thoroughly examined, revealing no significant differences between the fresh and reused catalysts. These results highlight the potential of functionalized cobalt-based metal-organic frameworks as versatile and sustainable catalysts for broader organic reactions.